Sulphamylarylamino triazines



Patented M. 2, 1943 nammo mas Gaetano F. DAiello, Plttaileid, Mata, animor to. Electric Company, a corporation of New York Ne Drag. Application November 28, 1941,

' Serial No. 420,861

l5 @s. (Cl. 280-248) This invention relate to new chemicalcommunds and more particularly to triazine de-' rivatives. The invention is concerned especially with the production of new and useful sulphamylarylao triazines.

The trleaine derivatives of this invention may i be represented graphically, by the iollowlng general formula:

1 (Rana -(un-z-s OgNHR) v ii In the above formula n represents an integer and is at least i and not more than 3, Z represents an aryl nucleus, and R represents a mem-- Mr of the class consisting of hydrogen and monovalent hydrocarbon and substituted by- ..drocarbon radicals, more particularly halohydrocarbon radicals. From a consideration of the formula it will be seen that when n is three there will be no amino (-NHR.) groups attached to the triazine nucleus.

Illustrative examples of monovalent radicals that R in the above tormula may represent are aliphatic (e. g., methyl, ethyl, propyl, isopropyl, ally], butyl, isobutyl, secondary butyl, butenyl,

l, isoamyl, hexyl, etc.), including cycloaliaha-tic (e. g., cyclopentyl, cyclopentenyl, cyclohenl, cyclohexenyl, cycloheptyl, etc.) aryl (e. g.; phenyl, diphenyl or xenyl, naphthyl, etc.); allphatic-substituted aryl (e. g.,toly'l, wlyl, ethylenyl, allylphenyl, E-butenylphenyl, propylphenyl, isopropylphenyl, .etc.); aryl-substituted aliphatic (e. a benzyl, phenyleth-yl, phenylpropyl,

The new chemical compounds-oi this invention may be used as pharmaceuticals. They are especially useful and valuable in the preparation I of synthetic resinous compositions, since they combine in one compound the advantages of theaminoarylsulphonamides and the triazlnes. Thus, they may be condensed with, for instance, aldehydes, including polymeric aldehydes and aldehydra-addition products; to yield condensation products of particular utility in the plastics and coating arts. Such condensation products are more fully described and are specifically claimed cinnamyl, etc); and their homologues, as well as those groups with one or more of their hydrogen atoms substituted by, for example, a halogen. examples of halo-hydrocarbon radicals are chlorcphenyl, chlorocyclohexyl, chloroethyl, dichiorophenyl, ethylchlorophenyl, phenylchloropropyl, bromobutyi, bromotolyl, etc. Preferably R is hydrogen.

Illustrative examples oi aryl nuclei that Z in Formula I may represent are: benzene; aliphaticsubstituted henzenes, e. s., the ortho-. metaand para-tcluenes, the xylenes, the etwlbenzenes, the propylbenzenes, etc.; the aromatic substituted benzenes, e. g., phenylbenzene, .etc.; naphthalene; the aliphatic-substituted naphthalenes, e. s the mono-, diand tri methyl naphthalenes, the mono-, diand trl-ethyl naphthalenes, the

mono-, diand tri-propyl naphthalenes, etc. the

in my ccpending application Serial No. 420,860, filed Nov. 28, 1941, and ed to the same assignee as the present invention.

Various methods may be employed to produce the chemical compounds of this invention, several oi. which are described below:

Mrrnon 1 This method comprises effecting reaction between a triamino .[(NHR):] triazine and an aminoarylsulphonamide. This reaction may be represented by the following general equation:

in an inert organic solvent having a boiling point above 0., for example ethylene glycol.

Illustrative examples of aminotriazines that may be used, depending upon the icular end- .products desired, are the ioliowiug M (NHR): symmetrical triazines (s-triazines):

2,4,6-triamino s-triazine 2.4-,6-tri-(methylamino) s-triazine 2,t,6-tri-(phenylamino) s-te htfi-tri-(chlorophenyll s-t e ZA-diamino e-ethylamino s-tre 2-amino 4,6-d;i-(benzylw o) s-triamne 2,4,6-tri- (allylamino) s-triamne ZA-diamino G-naphthylao s-trianne 2,d-dlamino 6-toluido s-trtm 2:0 4,6-di=(chlorophenyl ws-t azine QA-diamino G-chIorobutylw-a a I Illustrative examples of aminoarylsulphonamides that may be employed, depending upon the particular sulphamylarylamido substituent to be introduced into the triazine nucleus, are the following:

The aminonaphthalenesuIphonyl-chlorophenyl- 2 amides The aminobenzenesulphonyl-chlorobutylamides The aminobenzenesulphonyl-phenylethylamides The aminobenzenesulphonyl-propylphenylamides The following example illustrates the preparation of para-sulphamylanilino diamino s-triazine I by the above-described method. All parts are by weight.

Ems: 1 Parts Melamine 126 Suiphanilamide 172" The above' reactants were mixed and added to approximately 500 parts of ethylene glycol. The mixture was heated on an oilbath maintained at 160 C. for 6% hours and .then at 180 C. for

28% hours. The reaction vessel was provided with a reflux condenser which was so cooled that all the vapors except the ammonia evolved during the reaction were'condensed and returned to the vessel. After cooling, the reaction mass was poured into about 3,000 parts of cold water to precipitate the para-sulphamylanilino' diamino s-triazine resulting from the reaction. A yield of 178 parts of light brown crystals having a melting point of 250' to 255 C. was obtained. Subsequent recrystallization from hot water produced white crystals.

The following equation illustrates the above Another suitable method of preparing the novel 70 compounds of this invention comprises eifectingreaction between an aminoarylsulphonamide and ahalogenated s-triazine (that is, a triazine having a halogen atom attached directly to a carbon be representedby the following general equation:

I c s N N (arm) I! In the above equation X represents a halogen, and 11, Z and B. have the same meanings as given above with reference to Formula I.' This reaction advantageously is carried out in an anhydrous liquid medium, for example ether, benrene,

alcohol, etc. After the reaction has been completed and the crude product obtained, the latter is suitably treated to remove the hydrohalide, for example by washing with a dilute aqueous solution of a base such as sodium or potassium hydroxide.

Illustrative examples of halogenated s-triazines that may be used, depending upon the particular end-product sought. are listed below:

' 2-chloro 4,6-diamino s-triazine 2-bromo 4,6-diamino s-triazine 2,4-dichloro 6-amino s-triazine 2,4,6-trichloro s-triazine 2,4,6-tribromo s-triazine 2-iodo 4,6-diamino s-triazine 2-chlor0 4,8-di-(ethylamino) s-triazine 2,4-dichloro G-phenylamino s-triazine 2-chloro 4-ethylamino 6-amino s-triazine.

z-chloro 4-ethylamino G-phenylamino s-triazine 2-bromo 4,6-di-(cyclohexylamino) s-tflazine. 2-chloro 4,6-di-(chlorophenylamino) s-triazine 2-chloro 4-benzylamino B-amino s-triazine 2-chloro 4,6-di(toluido) s-triazine 7 Examples of aminoarylsulphonamides that may be used are-such as those mentioned above with reference to Method 1. Additional examples are arylsulphonamides such as mentioned in connection with Method 1 but wherein one of the 1B- drogen atoms of the amino grouping has been replaced by a hydrocarbon or halo-hydrocarbon radical, numerous examples of which radicals have been given above with reference to R of The following examples illustrate the preparation of chemicalcompounds of this invention in accordance with Method 2.

linux32 Preparation of para-sulphanwlanilino, diamino s'-triazine One mol of 2-chloro, its-ammo s-triasine and one moi of para-aminobenzenesulphonamida in ethylene gly l or other suitable anhydrous liquid medium are stirred together for from 15 to 24 hours at or below room temperature. The re-' action product (para-sulphamylanilino diamino s-triazine) is completely precipitated from the liquid medium by the additionof a liquid which is miscible with the anhydrom liquid medium but a non-solvent for the reaction product, e. g., ethyl alcohol. The product is washed free from nonvolatile contaminants and dried. The dried compound is stirred with a'dilute caustic solution, for

example a 5% sodium hydroxide solution, to free the amino or amido groups of the product from atom of the triazine nucleus). 'rhisreactl n ar (I my hydrochloride salt that may have formed during the reaction. The para-sulphamylanilino diamino s-triazine thus obtained may be purified further, if desired, by recrystallization from boiling water. Exams: 3

Preparation of 2,4,6-tri- (para-sulphcmylanilino) s-triazine i The same procedure is followed as described under Example 2 with the' exception that the halogenated triazine is 2,4,6-trichloro s-triazine and the para-aminobenzenesulphonamide is employed in an amount corresponding to 3 mole of the said sulphonamide per moi of the said halogenated triazine. This reaction may be .represented by the following equation:

NH-C uHq- S OrNHr The di-(sulphamylanilino) amino s-triazines are prepared in essentially the same manner as described under Example 2 using 2,4-dichloro amino s-triazine as a startingreactant and the proper molar. amount of the aminobenzenesulphonamide reactant. For example, di-(metasulphamylanilino) amino s-triazine is prepared by eflecting reaction as described under Example 2 between meta-aminobenaenesulphonamide and 2,4-d-ichloro amino s-triazine in the ratio of at least 2 mole of the former per moi of the latter.

The new chemical compounds of this invention, all of 'which contain at least one sulphamylarylamino group attached to the triazine nucleus, also may be prepared by causing a polyhalogenated s-triazine to react with an aminoarylsulphonamide in an amount insumclent to react with all of the halogen atoms of the halogenated triazine. The resulting product then is caused to react with ammonia or with an amine to yield various sulphamylarylamino s-triazines.

METHOD 3 Another method, which is applicable only to the preparation of tri-(sulphamylarylsmino) -subetituted triazines, involves the reaction of a cyanogen halide with an aminoarylsulphonamide. It is not known whether the reaction involves the reaction of the cyanogen halide with the aminosulphonamide as outlined under Method 2. The reaction may be represented by the following equation:

In the above equation X represents a halogen, and

Z and R. have the same meanings as given above with reference to Formula I.

M r-non 4 Another method which is especially suitable for use in preparing the newchemical compounds or this invention comprises effecting reaction between (1) an aminoarylsulphonamide having the general formula RHN-Z-SOzNHR, where R and Z have the same meanings as given above with reference to Formula I, and (2) a triazinyl aliphatic thioether selected from the class consisting of (a) mono-triazinyl aliphatic thioethers corresponding to the general formula II? N L where A represents a divalent aliphatic hydro- VII vnr

carbon radical selected from the class of radicalsrepresented by B and (B-O) m-B", where B and B represent divalent aliphatic hydrocarbon radicals, R has the same me as given above with reference to general Formula I, and m is a small integer, e. g., from 1 to 5. When a monotril aliphatic-thioether is used as a startins reactant, the reaction may be represented by the following general equation: 1

In Equations IX and x, A and A have the same meanings as given above with reference to Formulas VII and VIII, respectivelmand n (Equation IX), R and Z have the same meanings as given above with reference to Formula I. .The reactions represented by Equations 1x and X are best carried out in a solvent for the reactants, e. 3., a mixture of dioxane and water, and at the reflux temperature of the mass.

Illustrative examples of mono-triazinyl aliphatic thioethers that may be used, depending upon the particular product sought, are listed below:

Illustrative examples of bis-triazlnyl aliphatic thioethers that may be employed, depending upon the particular end-product desired, are shown below:

Alpha, beta-bis-(diamino s-triazinyl thio) ethane Alpha, gamma-bis- (diamino s-triazinyl thio) propane Y Alpha, omega-bis-(diamino s-triazinyl thio) butane Alpha, gamma-bis- [4,6 di (ethylamino) s-triazinyl-2 thiol propane Alpha, omeza-bis- [4,6-di-(anilino) s-triazinyl-2 thiol butane Beta, gamma-bis- [4,6 di (benzylamino) s-triazinyl-2 thio'l butane Alpha, beta-bis-(a-allylamino 6-chloroanilino striazinyl-2 thio) ethylene Alpha, alpha-bis-(i-toluido 6-amino s-triazinyl- 2.thio) ethane Beta, beta'-bis-(diamino s-triazinyl thio) diethyl ether l 1 Beta, beta bis (4 methylamino 6 naphthylamino s-triazinyl-2 thio) di-isopropyl ether Alpha, beta bis-(diamino s-triazinyl thio) ethylene Alpha, alpha bis (diamino s triazinyl thio) ethane Gamma, gamma'-bis-(diamino s-triazinyl thio) dipropyl ether Beta, beta'-bis-(diam.ino s-triazinyl thio) di-isobutyl ether Examples of aminoarylsulphonamides that may be used are such as those mentioned above with reference to Methods 1 and 2.

The following example illustrates the preparation of a novel chemical compound of this invention in accordance with Method 4. All parts are by weight.

Exam?- 1.:4

Preparation of para-sulphamylanilino diaminos-triazine I Approx. PM molntio Beta, beta'-bis-(diamiuo striasinyl thio) v diethylether 11.5 1 Para-aminobenzenesul phonamide ll. 0 2

The above components were dissolved in a boiling solution of equal parts dioxane and water. The solution was heated under reflux at the boiling temperature of the mass for 13 hours. At the end of the reaction period Just enough warm water was added to the hot reaction mass to cause incipient crystallization to take place. After cooling the mass to room temperature, the crude product (para-sulphamylanilino diamino s-triazine) was filtered oil. A purified material having a melting point of 253 C. was obtained by recrystallizing the crude product from a hot mixture of dioxane and water. I

The following equation representsv the reaction:

Meta-sulphamylanilino diamino s-triazine is producedas described above with reference to the production of para-sulphamylanilino diamino s-triazine with the exception that meta-aminobenzene sulphonamide is used as a starting reactant instead of para-aminob'enzenesulphonamide.

It will be noted that in the reaction represented by Equation XI a mono-(sulphamylarylamino) diamino s-triazine, specifically para-sulphamylanilino diamino s-triazine, is prepared by efl'ecting reaction between an aminoarylsulphonamide.

more particularly para aminobenzenesulphonamide, and a symmetrical bis-(diamino s-triazinyl thio) dialkyl ether, specifically beta, betabis-(diamino s-triazinyl thio) diethyl ether, in the ratio of at least two mols of the former to one mol or the latter.

From the foregoingdescription it will be seen that the present invention provides new and useful sulphamylarylamino triazines, examples of which are the tri-(sulphamylarylamino) striazines, the monoamino -NHR.) di-(sulphamylarylamino) s-triazines and the diamino [(-NHR)2] mono-(sulphamylarylamino) s-triazines. Other and more specific examples of these newacompounds are listed below:

Ortho-sulphamylanilino diamino s-triazine Meta-sulphamylanilino diamino s-triazine Para-sulphoamyltoluido diamino s-triazine Z-(meta-sulphamyltoluido) 4,6-di-(ethylamino) s-triazine Di-(ortho-sulphamylanilino) amino s-triazine Di-(meta-sulphamylanilino) amino s-triazine Di-(para-sulphamylanilino) amino s-triazine 2,4 di (ortho sulphamylanilino) Di-(para-sulphamyltoluido) amino s-triazine 2,4.6-tri-(ortho-sulphamylanilino) s-triazine 2,4,6-tri-(meta-sulphamylanilino) s-triazine 2,4,6-tri-(para-sulphamylanilino) s-triazine 2,4,6-tri-(para-sulphamyltoluido) s-triazine 2,4,8-tri-(meta-sulphamylxylidino) s-triazine 2 (para sulphamyltoluido) 4,6 di (methylamino) s-triazine 2 [para (phenylsulphamyl). xylidinol- 4.6 iii-(aniline) s-triazine 2 [para (methylsulphamyl) benzylamino] d-methylamino S-amino s-triazine I 2 [para (benzylsulphaml) chloroanilino] 4-toluido G-benzylamino s-triazine 2 [para (tolylsulphamyl) ethylanilino] chloroenilino G-amino s-triazine 2 (4' sulphamylnaphthyl 1' amino 4,6

diamino s -triazine 2 [para sulphamylphenyl (methyl) -amlno] 4,6-diamino s-triazine 2 (ortho sulphamylanilino) 4 7 (3 butenylamino) 6-chlorobutylamino s-triazine 2 [meta sulphamyltolyl (phenyl) amino] 4 (ethyl chloroanilino) 6 (chlorobutyl anilino) s-triazine 6 methylamino s-triazine 2,4 di (meta sulphamylanilino) 6 anilino s-triazine 2A di (para sulphamyltoluido) 6 benzylamino s-triazine 2,4 di (para sulphamylxylidino) 6 chloro- In a manner similar to that described above with particular reference to the production of slllphamylarylamino 135- or symmetrical tri- (chloroamylarylamino 1,2,4- or asymmetrical triazines (a-triazines) and the 1,2,3- or vicinal-triazines (v-trlazines) may be prepared.

What I claim as newand desire to secure by" Letters Patent of the United States is:

1. Chemical compounds corresponding to the general formula where n represents an integer and is at least 1 and not more than 3, Z represents an aryl nucleus, and It represents a member oi the class consisting of hydrogen and monovalent hydrocarbon and halorhydrocarbon radicals.

2. Chemical compounds as in claim 1 wherein R represents hydr gen. I

8. Chemical compounds as in claim 1 wherein 2 represents a benzene nucleus.

where n represents an integer and is at least 1 and not more than 3, Zrepresents an aryl nucleus, and R. represents a member of the class consisting or hydrogen and monovalent hydrocarbon and halo-hydrocarbon radicals, said method comprising eflecting reaction between (1) an aminoarylsulphonamide corresponding to the general azines (s-triazines), the corresponding sulphformula RHN-Z-SOaNHR, where R. and Z have the meanings above given, and (2) a. triazinyl aliphatic thioether selected from the class consisting of (a) mono-triazinyl aliphatic thioethers corresponding to the general formula l l (snm jg -(s-A) i- J where A represents a monovalent aliphatic hydrocarbon radical, and n and R have the mean-' ings above given, and (b) bis-triazinyl aliphatic thioethers corresponding to the general formula represented by B and (BO-) B', where B and B' represent divalent aliphatic hydrocarbon radicals, m is a small integer and is at least 1, and R. has the meaning above given.

13. A method as in claim 12 wherein R represents hydrogen.

14. The method of preparing a mono-(sulphamylarylamino) diamino s-triazine which comprises eii'ecting reaction between an aminoaryltwo mols of the former to one mol of the latter.

GAETANO F. DALELI of the 

